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The effects of morphine on Parkinson’s-related genes PINK1 and PARK2

BACKGROUND: Parkinson’s disease (PD) continues to be an important neurological disorder. It is caused by the loss of dopaminergic neurons in the substantia nigra. Dopamine, the neurotransmitter produced from dopaminergic neurons, is a major precursor of endogenous morphine. There are approximately 1...

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Autores principales: Snyder, Christopher, Mantione, Kirk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026148/
https://www.ncbi.nlm.nih.gov/pubmed/24800761
http://dx.doi.org/10.12659/MSMBR.890557
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author Snyder, Christopher
Mantione, Kirk
author_facet Snyder, Christopher
Mantione, Kirk
author_sort Snyder, Christopher
collection PubMed
description BACKGROUND: Parkinson’s disease (PD) continues to be an important neurological disorder. It is caused by the loss of dopaminergic neurons in the substantia nigra. Dopamine, the neurotransmitter produced from dopaminergic neurons, is a major precursor of endogenous morphine. There are approximately 18 genes associated with PD; their roles have not yet been completely established. PARK2 is a gene that encodes for the protein parkin, and PINK1 is a gene that encodes for PTEN-induced putative kinase 1. MATERIAL/METHODS: Our objective was to determine if morphine treatment of HTB-11 cells affects the expression of PINK1 and PARK2. HTB-11 cells were treated with 10(−7) M morphine for 2 h and a microarray analysis was conducted. To verify the microarray analysis, 3 Q-PCR trials were run using 10(−6) M naloxone, morphine (10(−7) M), or a naloxone/morphine mix. RESULTS: In both the microarray analysis and the Q-PCR analysis, PARK2 was up-regulated and PINK1 was down-regulated. CONCLUSIONS: Morphine can affect the expression of PD-associated genes.
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spelling pubmed-40261482014-05-20 The effects of morphine on Parkinson’s-related genes PINK1 and PARK2 Snyder, Christopher Mantione, Kirk Med Sci Monit Basic Res Laboratory Research BACKGROUND: Parkinson’s disease (PD) continues to be an important neurological disorder. It is caused by the loss of dopaminergic neurons in the substantia nigra. Dopamine, the neurotransmitter produced from dopaminergic neurons, is a major precursor of endogenous morphine. There are approximately 18 genes associated with PD; their roles have not yet been completely established. PARK2 is a gene that encodes for the protein parkin, and PINK1 is a gene that encodes for PTEN-induced putative kinase 1. MATERIAL/METHODS: Our objective was to determine if morphine treatment of HTB-11 cells affects the expression of PINK1 and PARK2. HTB-11 cells were treated with 10(−7) M morphine for 2 h and a microarray analysis was conducted. To verify the microarray analysis, 3 Q-PCR trials were run using 10(−6) M naloxone, morphine (10(−7) M), or a naloxone/morphine mix. RESULTS: In both the microarray analysis and the Q-PCR analysis, PARK2 was up-regulated and PINK1 was down-regulated. CONCLUSIONS: Morphine can affect the expression of PD-associated genes. International Scientific Literature, Inc. 2014-05-07 /pmc/articles/PMC4026148/ /pubmed/24800761 http://dx.doi.org/10.12659/MSMBR.890557 Text en © Med Sci Monit, 2014 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License
spellingShingle Laboratory Research
Snyder, Christopher
Mantione, Kirk
The effects of morphine on Parkinson’s-related genes PINK1 and PARK2
title The effects of morphine on Parkinson’s-related genes PINK1 and PARK2
title_full The effects of morphine on Parkinson’s-related genes PINK1 and PARK2
title_fullStr The effects of morphine on Parkinson’s-related genes PINK1 and PARK2
title_full_unstemmed The effects of morphine on Parkinson’s-related genes PINK1 and PARK2
title_short The effects of morphine on Parkinson’s-related genes PINK1 and PARK2
title_sort effects of morphine on parkinson’s-related genes pink1 and park2
topic Laboratory Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026148/
https://www.ncbi.nlm.nih.gov/pubmed/24800761
http://dx.doi.org/10.12659/MSMBR.890557
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